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LGI1 information


LGI1
Identifiers
AliasesLGI1, ADLTE, ADPAEF, ADPEAF, EPITEMPIN, EPT, ETL1, IB1099, leucine-rich, glioma inactivated 1, leucine rich glioma inactivated 1
External IDsOMIM: 604619; MGI: 1861691; HomoloGene: 3737; GeneCards: LGI1; OMA:LGI1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001308275
NM_001308276
NM_005097

NM_020278

RefSeq (protein)

NP_001295204
NP_001295205
NP_005088

NP_064674

Location (UCSC)Chr 10: 93.76 – 93.81 MbChr 19: 38.25 – 38.3 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Leucine-rich, glioma inactivated 1, also known as LGI1, is a protein which in humans is encoded by the LGI1 gene.[5] It may be a metastasis suppressor.

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000108231 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000067242 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Cite error: The named reference entrez was invoked but never defined (see the help page).

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Leucine-rich, glioma inactivated 1, also known as LGI1, is a protein which in humans is encoded by the LGI1 gene. It may be a metastasis suppressor. The leucine-rich...

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that form a complex with VGKC called leucine-rich glioma-inactivated 1 (LGI1) and contactin-associated protein-like 2 (CASPR-2). Each of these antibodies...

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RA, Fukata M (September 2006). "Epilepsy-related ligand/receptor complex LGI1 and ADAM22 regulate synaptic transmission". Science. 313 (5794): 1792–5....

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encephalitis Brain Various, depending on subtype (e.g., NMDA receptor antibodies, LGI1 antibodies) Confirmed Rare Balo concentric sclerosis Central nervous system...

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GRIK5 GRIN2A GRIN2B GRIN2C HER2/neu HGS KCNA2 KCNA4 KCNA5 KCNJ12 Kir2.1 LGI1 LRP1 LRP2 NLGN1 NOS1 PTK2B SEMA4C and SHANK2. Postsynaptic density GRCh38:...

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phonologic processing in familial lateral temporal lobe epilepsy due to a new LGI1 mutation". Epilepsia. 46 (1): 118–23. doi:10.1111/j.0013-9580.2005.26304...

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myasthenia gravis, and glycine receptors or potassium channel-associated proteins LGI1, CASPR2 and Contactin-2 in CNS diseases. She demonstrated that transfer of...

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Grzeschik KH, Derst C, Brodtkorb E, de Vos R, Steinlein OK (May 2002). "The LGI1 gene involved in lateral temporal lobe epilepsy belongs to a new subfamily...

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Autosomal dominant partial epilepsy with auditory features

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generalized seizures This disorder is caused by mutations in either the LGI1 gene or the RELN gene. These mutations are inherited in an autosomal dominant...

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type 4; 610353; CHRNA2 Epilepsy, partial, with auditory features; 600512; LGI1 Epilepsy, progressive myoclonic 1; 254800; CSTB Epilepsy, progressive myoclonic...

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